Canonical Allele Identifier: CA392337020
Community Standard Title: NM_000138.5(FBN1):c.6253T>A (p.Cys2085Ser)
Gene: FBN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48437828A>T , CM000677.2:g.48437828A>T GRCh38
NC_000015.9:g.48730025A>T , CM000677.1:g.48730025A>T GRCh37
NC_000015.8:g.46517317A>T NCBI36
NG_008805.2:g.212961T>A , LRG_778:g.212961T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000138.5:c.6253T>A MANE Select NP_000129.3:p.Cys2085Ser
ENST00000316623.10:c.6253T>A MANE Select ENSP00000325527.5:p.Cys2085Ser
NM_000138.4:c.6253T>A , LRG_778t1:c.6253T>A NP_000129.3:p.Cys2085Ser
ENST00000316623.9:c.6253T>A ENSP00000325527.5:p.Cys2085Ser
ENST00000537463.6:c.*2016T>A ENSP00000440294.2:n.*2016T>A
ENST00000559133.5:c.1560T>A
ENST00000559133.6:c.6253T>A ENSP00000453958.2:p.Cys2085Ser
ENST00000560820.1:n.373T>A
ENST00000674301.1:c.1252T>A ENSP00000501333.1:p.Cys418Ser
ENST00000674301.2:c.6253T>A ENSP00000501333.2:p.Cys2085Ser